Near-infrared (NIR) spectroscopy has been employed to investigate the evolution of the vibrational spectrum of water entrapped in a tricalcium silicate paste. The overall free water, which decreases as a function of time due to the formation of the hydrated phases (portlandite, Ca(OH)(2), and hydrated calcium silicate, C-S-H) during the hydration reaction, is quantified by the decrease in the area of the NIR band at about 5000 cm(-1). The coexistence of two types of water in the hydrated phases ( a "surface-interacting water" (type I) and a "bulklike water" (type II)) during the hydration is obtained by the analysis of the band at about 7000 cm(-1). The deconvolution of this band allows the quantification of the two water types. As the reaction advances, part of the "bulklike water" is converted to "surface- interacting water" in direct agreement with the C-S-H surface development. Finally, the Ca(OH)(2) formation can be concurrently monitored by NIR through the increase of a very sharp peak at 7083 cm(-1). Near-infrared spectroscopy allows determination in a very simple way of the most important features of the tricalcium silicate setting process.

NIR investigation of the water confined into tricalcium silicate pastes / F. RIDI; E. FRATINI; S. MILANI; P. BAGLIONI. - In: JOURNAL OF PHYSICAL CHEMISTRY. B, CONDENSED MATTER, MATERIALS, SURFACES, INTERFACES & BIOPHYSICAL. - ISSN 1520-6106. - STAMPA. - 110:(2006), pp. 16326-16331. [10.1021/jp060026y]

NIR investigation of the water confined into tricalcium silicate pastes

RIDI, FRANCESCA;FRATINI, EMILIANO;MILANI, SILVIA;BAGLIONI, PIERO
2006

Abstract

Near-infrared (NIR) spectroscopy has been employed to investigate the evolution of the vibrational spectrum of water entrapped in a tricalcium silicate paste. The overall free water, which decreases as a function of time due to the formation of the hydrated phases (portlandite, Ca(OH)(2), and hydrated calcium silicate, C-S-H) during the hydration reaction, is quantified by the decrease in the area of the NIR band at about 5000 cm(-1). The coexistence of two types of water in the hydrated phases ( a "surface-interacting water" (type I) and a "bulklike water" (type II)) during the hydration is obtained by the analysis of the band at about 7000 cm(-1). The deconvolution of this band allows the quantification of the two water types. As the reaction advances, part of the "bulklike water" is converted to "surface- interacting water" in direct agreement with the C-S-H surface development. Finally, the Ca(OH)(2) formation can be concurrently monitored by NIR through the increase of a very sharp peak at 7083 cm(-1). Near-infrared spectroscopy allows determination in a very simple way of the most important features of the tricalcium silicate setting process.
2006
110
16326
16331
F. RIDI; E. FRATINI; S. MILANI; P. BAGLIONI
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/252506
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